We’re looking for a Medical Writer to help create and review regulatory documents including protocols, informed consent forms, and clinical summaries. You’ll work with our team to transform data into clear, publication-ready content on realistic timelines.
What you’ll do:
Develop and review regulatory documentation, communicate with subject matter experts and external collaborators, manage document versions and timelines, and ensure all content meets regulatory standards.
Skills/background needed:
Strong writing and organisational skills, familiarity with reference management and graphic design tools (training provided), and a background in life sciences, healthcare, or a related field. No prior medical writing experience required—we’ll train you on regulatory requirements and best practices.
Contract length: Full time, ongoing
Rate: Competitive entry-level pay, details shared upon application.
Location: Remote work worldwide (English speaking preferred)
Ready to get started? Submit your application below.